Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene-Reference-Cited by-同舟云学术

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Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

Published:2000-11-14 Issue:9 Volume:55 Page:1267-1270
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Blumen S. C.,Korczyn A. D.,Lavoie H.,Medynski S.,Chapman J.,Asherov A.,Nisipeanu P.,Inzelberg R.,Carasso R. L.,Bouchard J.-P.,Tome F. M. S.,Rouleau G. A.,Brais B.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 44 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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3. The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy;Annals of Clinical and Translational Neurology;2023-01-23

4. Quantitative vs qualitative muscle MRI: Imaging biomarker in patients with Oculopharyngeal Muscular Dystrophy (OPMD);Neuromuscular Disorders;2023-01

5. Oculopharyngeal Muscular Dystrophy;Current Clinical Neurology;2023

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